Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | N-methoxy-N-methylpyridazine-3-carboxamide | HCID 58197546 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(Pyridazin-3-yl)ethan-1-ol | HCID 15197511 | 35% |
Reaction Steps
To a solution of compound 2 (300 mg, 0.6 mmol) in THF (15 mL) was added AcOH (1 mL) and H2O2 (3 mL). The reaction mixture was stirred at 30° C. for 10 h. The mixture was quenched with saturated NaHCO3 (6 mL) and then balanced between EtOAc (2×20 mL) and water (10 mL). The organic layers were collected and concentrated in vacuo to give the residue, which was purified by preparative TLC (petroleum ether:ethyl acetate=1:1) to give compound 3 (70 mg, 35%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09212153B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-54193b004b7548258da793e121d1e478 |
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| Source note | uspto-grants-2015_12 |
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